rs12061601, None

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
QT interval feature (observable entity)
CUI: C0429028
Disease: QT interval feature (observable entity)
226 1.000 0.040 1 169101212 intron variant T/C snv 0.16 0.800 1.000 3 2012 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 1.000 0.040 1 169101212 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 1.000 0.040 1 169101212 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012